نتائج البحث

A double CYP27A1 gene mutation in spinal cerebrotendinous xanthomatosis in a patient presenting with spastic gait: a case report.

• Authors : Min JH; Department of Neurology, Ajou University School of Medicine, Ajou University Medical Center, 164, World Cup-Ro, Yeongtong-Gu, Suwon, Republic of Korea.; Kim YS

Subjects: Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/genetics ; Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/drug therapy ; Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/Xanthomatosis, Cerebrotendinous*/diagnosis

• Source: Journal of medical case reports [J Med Case Rep] 2024 Jul 11; Vol. 18 (1), pp. 334. Date of Electronic Publication: 2024 Jul 11.Publisher: BioMed Central Country of Publication: England NLM ID: 101293382 Publication Model: Electronic Cited Medium: Internet ISSN: 1752-1947

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Highly selective motor nerve block and movement analysis for preoperative evaluation of complex spastic gait.

• Authors : Sanders JC; Shriners Hospitals for Children, Salt Lake City, UT, USA.; Department of Anesthesiology and Critical Care Medicine, University of New Mexico School of Medicine, Albuquerque, NM, USA.

Subjects: Gait Analysis* ; Denervation* ; Muscle Spasticity*/Muscle Spasticity*/Muscle Spasticity*/surgery

• Source: NeuroRehabilitation [NeuroRehabilitation] 2023; Vol. 53 (1), pp. 131-141.Publisher: IOS Press Country of Publication: Netherlands NLM ID: 9113791 Publication Model: Print Cited Medium: Internet ISSN: 1878-6448

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Vitamin D 3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis.

• Authors : Ehnert S; Siegfried Weller Research Institute at the BG Unfallklinik Tübingen, Department of Trauma and Reconstructive Surgery, University of Tübingen, Schnarrenbergstr. 95, 72076, Tübingen, Germany.; Hauser S

Subjects: Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/genetics ; Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/metabolism ; Oxysterols*

• Source: Scientific reports [Sci Rep] 2024 Mar 27; Vol. 14 (1), pp. 7335. Date of Electronic Publication: 2024 Mar 27.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Definitive radiotherapy for meningeal brainstem melanocytoma: a case report.

• Authors : Fernandez C; Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA, USA.; Hoeltzel G

Subjects: Melanoma*/Melanoma*/Melanoma*/radiotherapy ; Melanoma*/Melanoma*/Melanoma*/surgery ; Meningeal Neoplasms*/Meningeal Neoplasms*/Meningeal Neoplasms*/diagnostic imaging

• Source: British journal of neurosurgery [Br J Neurosurg] 2023 Oct; Vol. 37 (5), pp. 1307-1310. Date of Electronic Publication: 2020 Dec 26.Publisher: Taylor & Francis Country of Publication: England NLM ID: 8800054 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Dysfunctional neuro-muscular mechanisms explain gradual gait changes in prodromal spastic paraplegia.

• Authors : Lassmann C; Multi-level Modeling in Motor Control and Rehabilitation Robotics, Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany. .; Section Computational Sensomotorics, Hertie Institute for Clinical Brain Research, University of Tuebingen, Tuebingen, Germany. .

Subjects: Reflex, Abnormal* ; Paraplegia*; Humans Spastic Paraplegia Type 4

• Source: Journal of neuroengineering and rehabilitation [J Neuroeng Rehabil] 2023 Jul 15; Vol. 20 (1), pp. 90. Date of Electronic Publication: 2023 Jul 15.Publisher: BioMed Central Country of Publication: England NLM ID: 101232233 Publication Model: Electronic Cited Medium: Internet ISSN: 1743-0003

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Intramedullary Spinal Cord Abscess with Concomitant Spinal Degenerative Diseases: A Case Report and Systematic Literature Review.

• Authors : Jabbar R; Department of Neurosurgery, Spine and Peripheral Nerves Surgery, Medical University of Lodz, 90-549 Lodz, Poland.; Szmyd B

• Source: Journal of clinical medicine [J Clin Med] 2022 Aug 31; Vol. 11 (17). Date of Electronic Publication: 2022 Aug 31.Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101606588 Publication Model: Electronic Cited Medium: Print ISSN: 2077-0383

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Robot Assisted Gait Training in a Patient with Ataxia.

• Authors : Lamberti G; Spinal Unit, Azienda Usl, 29121 Piacenza, Italy.; Degree Course of Physiotherapy, University of Parma-Piacenza Training Center, Viale Abruzzo 12, 29017 Fiorenzuola d'Arda, Italy.

• Source: Neurology international [Neurol Int] 2022 Jun 22; Vol. 14 (3), pp. 561-573. Date of Electronic Publication: 2022 Jun 22.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551564 Publication Model: Electronic Cited Medium: Print ISSN: 2035-8385 (Print)

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Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early-onset psychosis.

• Authors : Alecu JE; Department of Neurology and F.M. Kirby Neurobiology Center, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; Saffari A

Subjects: Psychotic Disorders*/Psychotic Disorders*/Psychotic Disorders*/genetics ; Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/genetics; Adolescent

• Source: Annals of clinical and translational neurology [Ann Clin Transl Neurol] 2022 Apr; Vol. 9 (4), pp. 570-576. Date of Electronic Publication: 2022 Mar 16.Publisher: Wiley Periodicals, Inc on behalf of American Neurological Association Country of Publication: United States NLM ID: 101623278 Publication Model:

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An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions.

• Authors : Hayakawa M; Department of Pediatrics, Tokyo Metropolitan Kita Medical and Rehabilitation Center for the Disabled, 1-2-3 Jujodai Kita-ku, Tokyo, 114-0033, Japan.; Matsubara T

Subjects: Corpus Callosum* ; Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/genetics; Adolescent

• Source: BMC neurology [BMC Neurol] 2022 Jan 03; Vol. 22 (1), pp. 2. Date of Electronic Publication: 2022 Jan 03.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation: A Novel DARS2 Mutation and Intra-Familial Heterogeneity.

• Authors : Li JL; Department of Neurology National Taiwan University Hospital Taipei Taiwan.; Lee NC

• Source: Movement disorders clinical practice [Mov Disord Clin Pract] 2021 Aug 11; Vol. 8 (7), pp. 1116-1122. Date of Electronic Publication: 2021 Aug 11 (Print Publication: 2021).Publisher: Wiley Country of Publication: United States NLM ID: 101630279 Publication Model: eCollection Cited Medium: Internet ISSN: 2330-1619

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